In scientific writing services, we prepare non-clinical and clinical trial documents that effectively and clearly describe research results, product use, and other medical information.
We are a team of highly qualified professionals with having comprehensive understanding of clinical trial lifecycle and drug safety with expertise in multiple therapeutic areas.
We can assist your organization with the following strategic services which include regulatory medical writing, pharmacovigilance as well as scientific communications.
Regulatory Scientific writing
- Common Technical Document (Module 2.4, 2.5. 2.6 and 2.7)
- Integrated Summaries of Efficacy and Safety
- Clinical Study Reports – Phases I to IV
- Clinical Trial Protocols and Investigator Brochures
- Therapeutic justification
- Product Information for Prescriber and consumer
Publication and Literature Review
- Original Research Work (Clinical and Non-clinical)
- Systematic Review, Meta-analysis and Review Article
- Literature Review and References
Clinical Trial disclosure documents
- Synopses for public disclosure
- Protocol and Results Disclosure to Clinicaltrials.gov, EudraCT, and Local Registries
